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A Single Acidic Residue Can Guide Binding Site Selection but Does Not Govern QacR Cationic-Drug Affinity
- Kate M. Peters,
- Benjamin E. Brooks,
- Maria A. Schumacher,
- Ronald A. Skurray,
- Richard G. Brennan,
- Melissa H. Brown
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- Published: January 17, 2011
- https://doi.org/10.1371/journal.pone.0015974